1996
DOI: 10.1002/(sici)1099-0534(1996)8:1<63::aid-cmr5>3.3.co;2-l
|View full text |Cite
|
Sign up to set email alerts
|

Nuclear electric quadrupole relaxation

Abstract: Nuclei with spin quantum number I 1 have an asymmetric charge distribution and thus possess an electric quadrupole moment eQ. The interaction of the electric quadrupole moment with the electric field gradient of the bonding electrons provides the dominant relaxation mechanism of the quadrupolar nuclei, which are approximately three-quarters of the naturally occurring magnetic nuclei. This review summarizes the basic principles of nuclear electric quadrupolar relaxation. Particular emphasis is given to the effe… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

2
55
0
3

Year Published

2002
2002
2022
2022

Publication Types

Select...
9

Relationship

0
9

Authors

Journals

citations
Cited by 38 publications
(60 citation statements)
references
References 0 publications
2
55
0
3
Order By: Relevance
“…This is surprising, because oxygen and oxidation processes are at the heart of organic processes. This characterization technique, which is reputed to be very sensitive to electronic and steric environments, has been notably well developed in other fields of chemistry despite the relatively low abundance of 17 O (0.04 % on earth). A selection of 100 ubiquitous organic compounds, including notorious HFIP and TFE, is thus herein revisited by 17 O NMR spectroscopy with the aim of revealing what makes those oxofluorinated solvents so special.…”
Section: Methodsmentioning
confidence: 99%
“…This is surprising, because oxygen and oxidation processes are at the heart of organic processes. This characterization technique, which is reputed to be very sensitive to electronic and steric environments, has been notably well developed in other fields of chemistry despite the relatively low abundance of 17 O (0.04 % on earth). A selection of 100 ubiquitous organic compounds, including notorious HFIP and TFE, is thus herein revisited by 17 O NMR spectroscopy with the aim of revealing what makes those oxofluorinated solvents so special.…”
Section: Methodsmentioning
confidence: 99%
“…As in proton spectra, the precise chemical shift of a nucleus depends on the atom or atoms attached to it and there are correlations with the electronegativity of substituents. Because of the greater range of chemical shifts, 13 C spectra usually contain a separate resonance for each chemically shifted nucleus in the molecule (very little overlap of resonances occurs) (Banwell, 1994 (Gerothanassis & Tsanaktsidis, 1996;Gerothanassis, 1999;Rehder, 1999 (Figure 9, Gerothanassis, 1995;Gerothanassis & Kalodimos, 1996;Gerothanassis, 1999).…”
Section: The Case Of 13 Cmentioning
confidence: 99%
“…For instance, advanced pulse sequences yield 17 O NMR spectra with minimal baseline distortion and quadrupole central transition spectroscopy has recently been shown to provide high‐resolution 17 O NMR spectra for large protein‐ligand complexes in aqueous solution . 17 O NMR has been comprehensively reviewed by Gerothanassis in 2010, and not surprisingly, it appears that DNMR is seldom used. Reported 17 O DNMR studies mainly concern the exchange of metal‐coordinated water molecules using 17 O‐enriched water.…”
Section: Introductionmentioning
confidence: 99%